Canonical Allele Identifier: CA210258
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217597
dbSNP Id: rs779823379
gnomAD v2: 4-15581669-C-T
gnomAD v3: 4-15580046-C-T
gnomAD v4: 4-15580046-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15580046C>T , CM000666.2:g.15580046C>T GRCh38
NC_000004.11:g.15581669C>T , CM000666.1:g.15581669C>T GRCh37
NC_000004.10:g.15190767C>T NCBI36
NG_013035.1:g.115181C>T , LRG_697:g.115181C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389652.11:c.3886C>T ENSP00000374303.8:p.Arg1296Cys
ENST00000424120.6:c.3850C>T MANE Select ENSP00000403465.1:p.Arg1284Cys
ENST00000503292.6:c.3850C>T ENSP00000421809.1:p.Arg1284Cys
ENST00000506643.5:c.3703C>T ENSP00000422931.2:p.Arg1235Cys
ENST00000514039.6:c.79C>T ENSP00000488534.2:p.Arg27Cys
ENST00000634028.2:c.3703C>T ENSP00000488669.2:p.Arg1235Cys
ENST00000650860.2:c.*1347C>T ENSP00000498775.1:n.*1347C>T
ENST00000674945.1:c.3526C>T ENSP00000502333.1:p.Arg1176Cys
ENST00000675619.1:n.4682C>T
ENST00000675768.1:n.1070C>T
ENST00000676337.1:c.*856C>T ENSP00000501728.1:n.*856C>T
ENST00000680586.1:n.4509C>T
ENST00000389652.9:c.3348C>T
ENST00000424120.5:c.3850C>T ENSP00000403465.1:p.Arg1284Cys
ENST00000503292.5:c.3850C>T ENSP00000421809.1:p.Arg1284Cys
ENST00000506643.4:c.2178C>T
ENST00000634028.1:c.3656C>T ENSP00000488669.1:n.3656C>T
NM_001080522.2:c.3850C>T , LRG_697t1:c.3850C>T NP_001073991.2:p.Arg1284Cys
XM_005248177.1:c.3850C>T XP_005248234.1:p.Arg1284Cys
XM_011513869.1:c.3850C>T XP_011512171.1:p.Arg1284Cys
XM_011513870.1:c.3850C>T XP_011512172.1:p.Arg1284Cys
XM_011513871.1:c.3703C>T XP_011512173.1:p.Arg1235Cys
XM_017008482.1:c.3703C>T XP_016863971.1:p.Arg1235Cys
XR_001741296.1:n.4095C>T
NM_001378615.1:c.3850C>T MANE Select NP_001365544.1:p.Arg1284Cys
NM_001378617.1:c.3703C>T NP_001365546.1:p.Arg1235Cys